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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
---|---|
2018 | 2 |
2019 | 2 |
2020 | 1 |
2021 | 1 |
2022 | 1 |
2023 | 1 |
2024 | 0 |
Search Results
7 results
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Page 1
Editorial: Insights in pediatric endocrinology: 2022.
Front Endocrinol (Lausanne). 2023 Jun 14;14:1233451. doi: 10.3389/fendo.2023.1233451. eCollection 2023.
Front Endocrinol (Lausanne). 2023.
PMID: 37388213
Free PMC article.
No abstract available.
Editorial: Insights in pediatric Endocrinology: 2021.
Radovick S, Misra M.
Radovick S, et al.
Front Endocrinol (Lausanne). 2022 Jul 25;13:977912. doi: 10.3389/fendo.2022.977912. eCollection 2022.
Front Endocrinol (Lausanne). 2022.
PMID: 35957814
Free PMC article.
No abstract available.
Item in Clipboard
The Role of Insulin-like Growth Factor-1 (IGF-1) in the Control of Neuroendocrine Regulation of Growth.
Al-Samerria S, Radovick S.
Al-Samerria S, et al.
Cells. 2021 Oct 5;10(10):2664. doi: 10.3390/cells10102664.
Cells. 2021.
PMID: 34685644
Free PMC article.
Review.
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DLG2 variants in patients with pubertal disorders.
Jee YH, Won S, Lui JC, Jennings M, Whalen P, Yue S, Temnycky AG, Barnes KM, Cheetham T, Boden MG, Radovick S, Quinton R, Leschek EW, Aguilera G, Yanovski JA, Seminara SB, Crowley WF, Delaney A, Roche KW, Baron J.
Jee YH, et al.
Genet Med. 2020 Aug;22(8):1329-1337. doi: 10.1038/s41436-020-0803-8. Epub 2020 Apr 28.
Genet Med. 2020.
PMID: 32341572
Free PMC article.
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Genetic regulation of linear growth.
Yue S, Whalen P, Jee YH.
Yue S, et al.
Ann Pediatr Endocrinol Metab. 2019 Mar;24(1):2-14. doi: 10.6065/apem.2019.24.1.2. Epub 2019 Mar 31.
Ann Pediatr Endocrinol Metab. 2019.
PMID: 30943674
Free PMC article.
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QRICH1 mutations cause a chondrodysplasia with developmental delay.
Lui JC, Jee YH, Lee A, Yue S, Wagner J, Donnelly DE, Vogt KS, Baron J.
Lui JC, et al.
Clin Genet. 2019 Jan;95(1):160-164. doi: 10.1111/cge.13457. Epub 2018 Oct 26.
Clin Genet. 2019.
PMID: 30281152
Free PMC article.
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Ezh2 Mutations Found in the Weaver Overgrowth Syndrome Cause a Partial Loss of H3K27 Histone Methyltransferase Activity.
Lui JC, Barnes KM, Dong L, Yue S, Graber E, Rapaport R, Dauber A, Nilsson O, Baron J.
Lui JC, et al.
J Clin Endocrinol Metab. 2018 Apr 1;103(4):1470-1478. doi: 10.1210/jc.2017-01948.
J Clin Endocrinol Metab. 2018.
PMID: 29244146
Free PMC article.
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